Run ID: ERR10796584
Sample name:
Date: 31-03-2023 11:11:57
Number of reads: 9006
Percentage reads mapped: 99.98
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.4 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
fbiC | 1305157 | p.Pro743Thr | missense_variant | 1.0 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472279 | n.434T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472615 | n.770C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.75 |
ndh | 2102657 | p.Asp129Gly | missense_variant | 1.0 |
PPE35 | 2169681 | p.Gly311Ala | missense_variant | 1.0 |